Radiolysis via radioactivity is not responsible for rapid methane oxidation in subterranean air

PLoS One. 2018 Nov 1;13(11):e0206506. doi: 10.1371/journal.pone.0206506. eCollection 2018.

Abstract

Atmospheric methane is rapidly lost when it enters humid subterranean critical and vadose zones (e.g., air in soils and caves). Because methane is a source of carbon and energy, it can be consumed by methanotrophic methane-oxidizing bacteria. As an additional subterranean sink, it has been hypothesized that methane is oxidized by natural radioactivity-induced radiolysis that produces energetic ions and radicals, which then trigger abiotic oxidation and consumption of methane within a few hours. Using controlled laboratory experiments, we tested whether radiolysis could rapidly oxidize methane in sealed air with different relative humidities while being exposed to elevated levels of radiation (more than 535 kBq m-3) from radon isotopes 222Rn and 220Rn (i.e., thoron). We found no evidence that radiolysis contributed to methane oxidation. In contrast, we observed the rapid loss of methane when moist soil was added to the same apparatus in the absence of elevated radon abundance. Together, our findings are consistent with the view that methane oxidizing bacteria are responsible for the widespread observations of methane depletion in subterranean environments. Further studies are needed on the ability of microbes to consume trace amounts of methane in poorly ventilated caves, even though the trophic and energetic benefits become marginal at very low partial pressures of methane.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Air / analysis*
  • Air Pollutants / analysis
  • Air Pollutants / metabolism
  • Air Pollutants / radiation effects
  • Caves / chemistry*
  • Environmental Monitoring
  • Methane / analysis
  • Methane / metabolism
  • Methane / radiation effects*
  • Oxidation-Reduction / radiation effects
  • Radioactivity*
  • Soil / chemistry*
  • Time Factors

Substances

  • Air Pollutants
  • Soil
  • Methane

Grants and funding

This study is based upon work at Indiana University supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division under Award Number DE-SC0006978 awarded to Arndt Schimmelmann. Work at the Royal Holloway University of London (RHUL) was supported by the Spanish Ministry of Economy and Competitiveness projects CGL2016-78318-C2-1R and CGL2016-78318-C2-2R AEI/FEDER/UE awarded to Angel Fernandez-Cortes. Jay T. Lennon was supported by the U.S. National Science Foundation (1442246) and the U.S. Army Research Office (W911NF-14-1- 0411). Jay T. Lennon further acknowledges support from the Indiana University Office of the Vice President of International Affairs. Angel Fernandez-Cortes' work was further supported by project SMACKS (IEF-Marie Curie Actions nº 624204, FP7/2007-2013). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.